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首页> 外文期刊>Journal of Pharmacy and Pharmacology >In-vitro and in-vivo evaluation of pH-responsive polymeric micelles in a photodynamic cancer therapy model.
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In-vitro and in-vivo evaluation of pH-responsive polymeric micelles in a photodynamic cancer therapy model.

机译:在光动力癌症治疗模型中对pH响应性聚合物胶束的体外和体内评估。

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摘要

pH-sensitive polymeric micelles of randomly and terminally alkylated N-isopropylacrylamide copolymers were prepared and characterized. Aluminium chloride phthalocyanine (AlClPc), a second generation sensitizer for the photodynamic therapy of cancer, was incorporated in the micelles by dialysis. Their photodynamic activities were evaluated in-vitro against EMT-6 mouse mammary tumour cells and in-vivo against EMT-6 tumours implanted intradermally on each hind thigh of Balb/c mice. pH-sensitive polymeric micelles were found to exhibit greater cytotoxicity in-vitro than control Cremophor EL formulations. In the presence of chloroquine, a weak base that raises the internal pH of acidic organelles, in-vitro experiments demonstrated the importance of endosomalllysosomal acidity for the pH-sensitive polymeric micelles to be fully effective. Biodistribution was assessed by fluorescence of tissue extracts after intravenous injection of 2 micromol kg(-1) AlClPc. The results revealed accumulation of AlClPc polymeric micelles in the liver, spleen and lungs, with a lower tumour uptake than AlClPc Cremophor EL formulations. However, polymeric micelles exhibited similar activity in-vivo to the control Cremophor EL formulations, demonstrating the higher potency of AlClPc polymeric micelles when localized in tumour tissue. It was concluded that polymeric micelles represent a good alternative to Cremophor EL preparations for the vectorization of hydrophobic drugs.
机译:制备并表征了无规和末端烷基化的N-异丙基丙烯酰胺共聚物的pH敏感聚合物胶束。通过透析将氯化铝酞菁(AlClPc)(用于癌症光动力疗法的第二代敏化剂)掺入胶束中。他们的光动力学活性在体外针对EMT-6小鼠乳腺肿瘤细胞进行了评估,并在体内针对经Balb / c小鼠后腿皮内植入的EMT-6肿瘤进行了评估。发现pH敏感的聚合物胶束比对照Cremophor EL制剂具有更大的体外细胞毒性。在氯喹(一种弱的碱,会升高酸性细胞器的内部pH)的存在下,体外实验表明,胞内溶酶体酸度对于pH敏感的聚合物胶束完全有效非常重要。通过静脉内注射2 micromol kg(-1)AlClPc后组织提取物的荧光来评估生物分布。结果表明,AlClPc聚合胶束在肝脏,脾脏和肺中积累,且肿瘤吸收率低于AlClPc Cremophor EL制剂。然而,聚合物胶束在体内表现出与对照Cremophor EL制剂相似的活性,证明了当位于肿瘤组织中时,AlClPc聚合物胶束的效力更高。结论是,聚合物胶束是Cremophor EL制剂用于疏水性药物载体化的良好替代品。

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